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Implements a kernel-based association test for copy number variation (CNV) aggregate analysis in a certain genomic region (e.g., gene set, chromosome, or genome) that is robust to the within-locus and across-locus etiological heterogeneity, and bypass the need to define a "locus" unit for CNVs. Brucker, A., et al. (2020) <doi:10.1101/666875>.
Package details |
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Author | Amanda Brucker, Shannon T. Holloway, Jung-Ying Tzeng |
Maintainer | Shannon T. Holloway <shannon.t.holloway@gmail.com> |
License | GPL-2 |
Version | 1.4 |
Package repository | View on CRAN |
Installation |
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